http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2718103-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c7ad58d3c0b071069a8ee0cb8c8ba2e8
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-76
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-86
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-76
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-72
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-86
filingDate 1977-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d899146c33731199955aedeea27f0641
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_90ccb9ede498b5469f5e17b6cf511644
publicationDate 1978-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2718103-A1
titleOfInvention PROCESS FOR THE PRODUCTION OF AMIDE GROUP MODIFIED (THIO) HYDANTOINS
abstract Amide gp-substd (thio)hydantoins are prepd. by (a) reacting maleimides having formula (I): (where R1 and R2 are H or an aliphatic gp. R5 is H or an opt. substd aliphatic, cycloaliphatic, aromatic, aliphatic-aromatic or heterocyclic gp. and k is 1-3, esp. 1-2) with a prim. mono- or polyamine (b) reacting the prod. with an organic mono- or polyiso (thio)cyanate and (c) cyclising by heating opt. in the presence of catalysts. Monohydantoins can be used as plant-protective agents or as pharmaceuticals. Poly(thio)hydantoins are heat-stable and used as lacquers(claimed), e.g. for metal sheets and wires, as adhesives, foils and mouldings. (A) can be built into polymers to increase heat-stability. (I) are prepd. smoothly and in high yields. In an example 1,3-diphenyl-5-(phenylaminocarbonyl-methylene)-hydantoin was prepd. by (i) reacting aniline and N-Ph maleimide, (ii) reacting prod. with PhNCO and (iii) cyclising.
priorityDate 1977-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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